Canonical Allele Identifier: PA2826262043
Gene: CRHR2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189411.1:p.Ile114Val
CA4206599
NM_001202482.2:c.340A>G